ClinVar Miner

List of variants in gene combination DCLRE1C, SUV39H2 reported as benign by Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001193424.2(SUV39H2):c.850-483T>G	rs7896464	0.41115
NM_001193424.2(SUV39H2):c.850-305C>T	rs60006238	0.08419

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